research-enabled Visit Centres. Orizzonte combines Central Research Operations,
robust governance and dedicated research capability to support consistent, high-quality study delivery.
Sponsors & CROs
Healthcare-integrated clinical research delivered through a network of research-enabled Visit Centres. Orizzonte combines Central Research Operations, robust governance and dedicated research capability to support consistent, high-quality study delivery.
A Different Approach to Research Delivery
Clinical research delivery continues to evolve alongside healthcare systems, participant expectations, and study requirements. While hospital-based research remains essential for many studies, selected research activities may also be delivered through community healthcare environments. Orizzonte’s infrastructure model extends research delivery into established healthcare settings through research-enabled Visit Centres supported by central operational management and governance frameworks.
Accelerated Recruitment
Improved Retention
Increased Diversity & Inclusion
Regulatory Confidence
Operational Efficiency
Why Partner with Orizzonte
Accelerated Recruitment
Improved Retention
Increased Diversity & Inclusion
Regulatory Confidence
Operational Efficiency
Why Partner with Orizzonte?
Orizzonte provides healthcare-integrated research infrastructure designed to support Sponsors and CROs throughout the study lifecycle.
Our model combines:
▪️ Research-enabled Visit Centres
▪️ Central Research Operations
▪️ Feasibility and site selection
▪️ Participant recruitment
▪️ Governance and quality oversight
▪️ Multi-site delivery
Why Partner with Orizzonte?
Orizzonte provides healthcare-integrated research infrastructure designed to support Sponsors and CROs throughout the study lifecycle.
Our model combines:
▪️ Research-enabled Visit Centres
▪️ Central Research Operations
▪️ Feasibility and site selection
▪️ Participant recruitment
▪️ Governance and quality oversight
▪️ Multi-site delivery
Visit Centres
Visit Centres integrate clinical research into established primary care.
Depending on study requirements, they may support:
▪️ Participant recruitment
▪️ Study visits
▪️ Study assessments
▪️ Follow-up appointments
▪️ Research coordination
Visit Centres
Visit Centres integrate clinical research into established primary care.
Depending on study requirements, they may support:
▪️ Participant recruitment
▪️ Study visits
▪️ Study assessments
▪️ Follow-up appointments
▪️ Research coordination
Central Research Operations
Central Research Operations coordinate study delivery across the network.
Core functions include:
▪️ Study start-up
▪️ Site activation
▪️ Operational planning
▪️ Sponsor communication
▪️ Quality oversight
▪️ Performance monitoring
Central Research Operations
Central Research Operations coordinate study delivery across the network.
Core functions include:
▪️ Study start-up
▪️ Site activation
▪️ Operational planning
▪️ Sponsor communication
▪️ Quality oversight
▪️ Performance monitoring
Feasibility & Site Selection
Every study is assessed to identify the most appropriate delivery model.
Assessments consider:
▪️ Protocol requirements
▪️ Participant populations
▪️ Infrastructure capability
▪️ Operational feasibility
▪️ Delivery complexity
Feasibility & Site Selection
Every study is assessed to identify the most appropriate delivery model.
Assessments consider:
▪️ Protocol requirements
▪️ Participant populations
▪️ Infrastructure capability
▪️ Operational feasibility
▪️ Delivery complexity
Governance & Quality
Research delivery is supported by centrally managed governance and quality systems.
These frameworks support:
▪️ Participant safety
▪️ Regulatory compliance
▪️ Data integrity
▪️ Consistent operational standards
Governance & Quality
Research delivery is supported by centrally managed governance and quality systems.
These frameworks support:
▪️ Participant safety
▪️ Regulatory compliance
▪️ Data integrity
▪️ Consistent operational standards
Empowering clinicians to become research-active is not just about advancing science — it’s about transforming care at its core
Dr. Aries Maximus Ogbuokiri
COO
Working With Orizzonte
Orizzonte works collaboratively with Sponsors and CROs to assess study requirements, delivery pathways, and infrastructure suitability.
The objective is to align each study with the most appropriate research environment while maintaining operational consistency and participant-focused delivery.
Frequently Asked Questions
Every opportunity is assessed individually based on protocol requirements, participant safety and operational feasibility.
Yes. Our centrally managed infrastructure is designed to support consistent delivery across multiple Visit Centres.
Site selection is based on feasibility, participant populations, infrastructure capability and study requirements.
Yes. We work directly with Sponsors and CROs from feasibility through to study delivery.
Frequently Asked Questions
Suitability depends on study requirements, participant safety considerations, infrastructure needs, and operational feasibility. Each opportunity is assessed individually.
Operational management, governance frameworks, and standardised processes support consistency across multiple Visit Centre locations.
Yes. The infrastructure model is designed to support commercial clinical research delivery alongside other study types where appropriate.
Site selection is informed by feasibility assessment, infrastructure capability, participant pathways, and operational requirements.
Yes. Orizzonte collaborates directly with Sponsors and CROs throughout feasibility, study planning, activation, and delivery.
Empowering clinicians to become research-active is not just about advancing science — it’s about transforming care at its core
Dr. Aries Maximus Ogbuokiri
COO
Discuss Your Study
Talk to our team about delivering your next study through Orizzonte’s healthcare-integrated research infrastructure.
Latest News & Articles
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The Diversity Dilemma: Why Representation in Clinical Trials Is Non-Negotiable
Decentralized Clinical Trials: Redefining Research in a Digitally Connected World
Connect with our leaders
Dr. Zuhaib Keekeebhai
Lead Principal Investigator – Primary Care Trials
Dr Gillian Hood
Diabetes Research Manager at Barts & the London School of Medicine and Dentistry, Queen Mary, University of London
Akash Patel
Consultant Trauma and Orthopaedic Surgeon at RoyalFreeLondonNHSFoundation Trust and Associate professor at University College London
Who we work with
Pharmaceuticals
Hospitals
Academia
Who we work with
Pharmaceuticals
Hospitals
Academia
Why It Matters
Reduced Trial Delays
Evidence-based site selection helps avoid underperforming sites and recruitment shortfalls.
Real-World Representation
Our network includes practices in urban, rural, and underserved regions—ensuring diversity in study populations.
Sponsor Confidence
Data-driven feasibility and operational readiness give sponsors the insight they need for confident site selection.
